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Biophys J, September 2000, p. 1228-1236, Vol. 79, No. 3
and
*Department of Molecular Evolution, Evolutionary Biology Centre,
and
Department of Cell and Molecular Biology, Biomedical
Center, Uppsala University, Uppsala, Sweden
Living cells differ from most other chemical systems in
that they involve regulation pathways that depend very nonlinearly on
chemical species that are present in low copy numbers per cell. This
leads to a variety of intracellular kinetic phenomena that elude
macroscopic modeling, which implicitly assumes that cells are
infinitely large and fluctuations negligible. It is of particular importance to assess how fluctuations affect regulation in cases where
precision and reliability are required. Here, taking finite cell size
and stochastic aspects into account, we reinvestigate theoretically the
mechanism of zero-order ultrasensitivity for covalent modification of
target enzymes (Goldbeter and Koshland (1981)
Proc. Natl. Acad. Sci. USA. 78:6840-6844). Macroscopically, this mechanism can produce a very sharp transition in target
concentrations for very small changes in the activity of the converter
enzymes. This study shows that the transition is much more gradual in a finite cell or a population of finite cells. It also demonstrates that
the switch is exactly analogous to a thermodynamic phase transition and
that ultrasensitivity is inevitably coupled to random ultravariation.
As a consequence, the average response in a large population of cells
will often be much more gradual than predicted from macroscopic descriptions.
Biophys J, September 2000, p. 1228-1236, Vol. 79, No. 3
© 2000 by the Biophysical Society 0006-3495/00/09/1228/09 $2.00
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